Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727503110
KRAS
0.882 0.160 12 25245320 missense variant T/A;C snv 3
rs80338799
RAF1
0.882 0.160 3 12585745 missense variant G/A;C snv 3
rs876657651
MAP2K1
0.882 0.160 15 66436818 missense variant A/G snv 3
rs1040124120
ZHX2
1.000 0.160 8 122953350 missense variant C/G;T snv 1.6E-05 2
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2
rs1114167651
PTEN
1.000 0.160 10 87933107 missense variant C/A;T snv 4.0E-06 2
rs1239105602
PTEN ; KLLN
1.000 0.160 10 87864168 5 prime UTR variant C/T snv 2
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 2
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2
rs267607080
SOS1
0.925 0.160 2 39023134 missense variant A/G snv 2
rs397507477
BRAF
1.000 0.160 7 140777995 missense variant G/A snv 2
rs397507504
PTPN11
0.925 0.160 12 112450346 missense variant A/G snv 7.0E-06 2
rs397507512
PTPN11
0.925 0.160 12 112450391 missense variant T/C;G snv 2
rs397507518
PTPN11
0.925 0.160 12 112450508 missense variant G/A snv 2
rs397507525
PTPN11
0.925 0.160 12 112472968 missense variant C/T snv 7.0E-06 2
rs397507543
PTPN11
0.925 0.160 12 112489078 missense variant G/A snv 2
rs397516801
PTPN11
0.925 0.160 12 112450389 missense variant A/G snv 2
rs397516810
PTPN11
0.925 0.160 12 112477652 missense variant T/G snv 2
rs397516815
RAF1
0.925 0.160 3 12585760 missense variant T/C snv 2
rs397516826
RAF1
0.925 0.160 3 12604202 missense variant C/A;G snv 2
rs397516828
RAF1
0.925 0.160 3 12604188 missense variant G/A;C snv 2
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 2
rs397517164
SOS1
0.925 0.160 2 39058696 missense variant C/T snv 2
rs397517166
SOS1
0.925 0.160 2 39058683 missense variant G/C snv 2
rs397517180
SOS1
0.925 0.160 2 39035440 missense variant C/A snv 2